Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96619763-96620021 | Common:2; Rare:111 | ||||
| chr9:96653821-96654680 | Common:4; Rare:203 | ||||
| chr9:96654790-96655117 | Common:5; Rare:178 | ||||
| chr9:96655179-96655475 | Common:3; Rare:208 | ||||
| chr9:96777968-96778182 | Common:1; Rare:140 | ||||
| chr9:96854255-96854678 | Common:9; Rare:250 | ||||
| chr9:96875836-96876082 | Rare:63 | ||||
| chr9:97013570-97013847 | Common:8; Rare:149 | ||||
| chr9:97039097-97039346 | Common:1; Rare:203 | ||||
| chr9:97411876-97412239 | Common:7; Rare:139; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:97501436-97501755 | Common:12; Rare:142 | ||||
| chr9:97632990-97633916 | Common:20; Rare:777 | ||||
| chr9:97675961-97676686 | Common:10; Rare:194 | ||||
| chr9:97696690-97697160 | Common:5; Rare:142; Clinvar:1 | ||||
| chr9:97697170-97697578 | Common:4; Rare:305; Clinvar:11; Clinvar (benign):2; Clinvar (pathogenic):4 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box